Establishment registration
JOIMAX GMBH
FDA establishment registration 3005083075 · KARLSRUHE Baden-Wurttemberg, DE
Key facts
| Registration number | 3005083075 |
|---|---|
| Establishment name | JOIMAX GMBH |
| Owner/operator | Joimax GmbH |
| Owner/operator number | 9070895 |
| FEI number | 3005083075 |
| Address | AMALIENBADSTRASSE 41 |
| City | KARLSRUHE Baden-Wurttemberg |
| Country | DE |
| Establishment types | Foreign private label distributor |
| Registration valid through | 2026 |
| Product codes listed | BWN, BZN, FFY, FQH, FSM, FTY, FWF, FZS, FZX, FZY, FZZ, GAA, GAC, GDC, GDF, GEG, GEI, GEN, GFI, HAO, HRR, HRX, HTO, HWE, HWJ, HXI, HXK, HXZ, KCT, KDD and 14 more |
| Device classes | 1, 2 |
At a glance
- 10–99 Device listings
- 1,000+ UDI devices (GUDID)
- Current Registration current
- 1–9 FDA inspections at this FEI
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA device establishment registrations
Device establishments that manufacture, repackage, relabel or import devices for the U.S. market must register annually with the FDA and list the devices they produce.
Source: U.S. Food and Drug Administration (FDA), Establishment Registration and Device Listing database